Clearance Summary
GASTROSTOMY FEEDING DEVICE received FDA 510(k) clearance under submission number K884439, sponsored by Southside Biotechnology. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1988-12-05.
- Submission: K884439
- Applicant / Sponsor: Southside Biotechnology
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5980
- Decision date: 1988-12-05
Classification & Regulation
This clearance is catalogued under FDA product code KNT and 21 CFR 876.5980, within the Gastroenterology, Urology review panel as a Class II device.